- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07111585
- Original Trial
Personalized Health Coaching for Patients With HF (Coach-FrailHF)
Effect of Personalized Health Coaching Program in Patients With Frailty and Heart Failure
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The prevalence of heart failure (HF) is increasing worldwide, and consistently in Korea, it has more than tripled between 2002 and 2020. As a result, the hospitalization rate due to HF has increased by 1.6 times, and the age-standardized mortality rate by more than fivefold. Despite the implementation of various treatment and management strategies, hospitalizations, unplanned visits and mortality related to HF continue to rise, underscoring the urgent need for multidimensional and personalized approaches to patient care. Particularly in Korea, the prevalence of HF begins to rise in an individual's 30s, and shows a significant increase after the age of 40s, with mortality rates gradually upward among middle-aged patients. Thus, there is the need to focus on health care among patients aged 40 and over.
One of the most common and critical issues observed in patients with HF is frailty. In HF, frailty is defined as a multidimensional, dynamic, and potentially reversible condition that, although age-related, is distinct from aging, that increases susceptibility to stressors and adverse outcomes. The overall prevalence of frailty among HF patients is estimated round 44.5%, although varying among measurement tools. Patients with frailty and HF exhibit a higher risk of cardiovascular death, HF-related hospitalization, all-cause death, and all-cause hospitalization as well as a lower quality of life (QoL). Although frailty is often age-related, it is not exclusive to the elderly, making frailty assessment essential for all patients with HF. Most existing frailty assessment tools emphasize only physical aspects and fail to capture the complexity of frailty in HF patients. Therefore, it is essential to plan and evaluate patients care using a multidimensional approach encompassing clinical, functional, cognitive-psychological, and social domains, as recommended by HF associations, which may help prevent or reduce adverse clinical outcomes.
According to the research results conducted so far, the evidence that multidimensional interventions more effectively improve frailty than single-domain interventions have been consisted, and a variety of healthcare professionals have delivered collaborative interventions to improve frailty. Among theses, nurse-led multidimensional interventions for community-dwelling older adults have shown improvements in frailty, physical function, nutritional status, QoL, social support, and mental health including reduced depression. In inpatient settings, nurses might play a key role in multidisciplinary teams as skilled health professional, educators, care coordinators, patient advocates, and liaisons. Therefore, HF nurses are able to plan and implement personalized interventions tailored to patients' individual needs in a central role.
The period from hospital admission to discharge is the most appropriate time to plan transition from hospital to home and a critical window for multidisciplinary intervention with HF patients. During hospitalization, above all else patients are at a high-risk stage of HF progress and frailty, and so early identification and fast management of HF progress are crucial. But most multidimensional interventions for frailty in HF have been conducted in community-based settings with no connection from the time of hospitalization. Hospital HF nurses can closely monitor patients' frailty status, coordinate with the care team, and plan for effective care transitions post-discharge. A structured transitional care strategy can help HF patients to maintain health care management and prevent readmissions at home.
Health coaching has emerged as an effective, goal-oriented, and patient-centered approach to support post-discharge self-care and behavior modification. After discharge interventions through phone calls, home visits, outpatient visit, or remote monitoring are essential components of HF management programs. A meta-analysis found that telecoaching has a significant impact on health outcomes, improving self-care and QoL in patients with HF. One study demonstrated that a 3-month personalized coaching program significantly reduced emergency visits and 6-month readmission rates, highlighting the importance of time in effecting behavioral change. Another study indicated that while younger patients prefer mobile or text-based interventions, older adults are more inclined to use telephone coaching in combination with paper-based health summaries. Thus, telephone coaching with paper manual book might be a particularly effective intervention for older, frail HF patients.
This study aims to present a protocol for evaluating the effects of a personalized telephone-based health coaching program on frailty, health-related QoL, and clinical outcomes among older patients hospitalized with heart failure. The findings are expected to contribute to the development of a practical, nurse-led inpatient intervention model that enhances the quality of HF patient care.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Wook-Jin Chung, MD
- Phone Number: 82-32-460-3663
- Email: heart@gilhospital.com
Study Locations
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Incheon, Korea, Republic of
- Recruiting
- Department of Cardiovascular Medicine, Gachon University, Gil Medical Center, Incheon,
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Contact:
- Jihye Yoon, MSN
- Phone Number: 82-32-460-3663
- Email: zhyeyun@gilhospital.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants aged 40 years or older will be included in the study, as heart failure (HF)-related mortality and the prevalence of HF increase significantly from this age onward. Inclusion criteria requires a diagnosis of acute HF by a cardiologist and hospitalization based on the following criteria: presence of HF symptoms (e.g., breathlessness, fatigue, ankle swelling) and signs (e.g., elevated jugular venous pressure, pulmonary crackles, peripheral edema), evidence of pulmonary congestion or edema on chest X-ray, and elevated levels of BNP (≥100 pg/mL) or NT-proBNP (≥300 pg/mL). After initial screening for frailty using both the Tilburg Frailty Indicator (TFI) and Fried's Phenotype (FP), participants will be enrolled if they are classified as frail, able to cooperate with functional assessments, and willing to provide written informed consent with a clear understanding of the study's purpose and procedures.
Exclusion Criteria:
- The exclusion criteria were as follows: current enrollment in other programs or planning to participate in similar programs during the intervention period; residing outside Korea and not understanding Korean; diagnosis of dementia with the Global Deterioration Scale stage of 5 or greater; inability to comprehend the study purpose and content.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Personalized health coaching program
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Clinical: Pre-discharge education on HF management (e.g., symptoms, treatment, diet, medication, lifestyle) is provided with a booklet and website link. A digital scale is given. After discharge, 12-week phone coaching monitors medication adherence, weight, and sodium intake. Functional: Patients are referred to cardiac rehab for tailored exercise plans. Education on home exercise and oxygen monitoring is provided, with QR-linked videos. Coaching supports exercise adherence. Psycho-cognitive: Emotional support is based on the PERMA model. Patients with severe issues are referred to psychiatry. Post-discharge, coaching includes psychiatric appointment support and use of the 100-Day Diary for self-care and gratitude journaling. Social: Nurses foster trust and social reintegration. Referrals to community services are made as needed. Weekly calls ensure service connection and address unmet needs via social workers. |
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Other: standard care
|
Participants in the control group will receive standard care, including guideline-directed medical therapy, based on the latest clinical guidelines currently provided to patients with HF at the hospital, as well as HF education.
HF education will be provided using a booklet that includes information on HF (definition, causes, symptoms, diagnosis, treatment, medications, and self-management), an exercise poster, a symptom log, a symptom checklist, fall prevention tips, and a dietary guide.
Additionally, nutritionist consultations on HF-related diets, cardiac rehabilitation exercises, and financial support available through the social work department, if necessary, will be provided.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical Frailty Scale (CFS)
Time Frame: Baseline assessment, Mid assessment (6 week), Post assessment (12 week), Final assessment (24 week)
|
The CFS measures frailty using a quick assessment through brief descriptions and illustrations.
The total score ranges from 1 to 9, with a score of ≥4 indicating frailty.
|
Baseline assessment, Mid assessment (6 week), Post assessment (12 week), Final assessment (24 week)
|
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Kansas City Cardiomyopathy Questionnaire clinical summary score (KCCQ-CSS)
Time Frame: Baseline assessment, Mid assessment (6 week), Post assessment (12 week), Final assessment (24 week)
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The Clinical Summary Score (CSS) is calculated as the mean of the Physical Limitation Score and the Total Symptom Score from the KCCQ.
The KCCQ CSS ranges from 0 to 100, where higher scores indicate better health status.
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Baseline assessment, Mid assessment (6 week), Post assessment (12 week), Final assessment (24 week)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Tilburg Frailty Indicator (TFI)
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
The TFI was developed based on an integral conceptual model of frailty that categorizes it into 3 dimensions: physical (8 items), psychological (4 items), and social (3 items).
The frailty score (maximum, 15) is determined by summing the scores of the 3 frailty domains.
Frailty is identified as a score ≥5.
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
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Frailty phenotype (FP)
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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The FP included the following 5 criteria: loss of muscular strength (grip strength), reduced gait speed, weight loss, exhaustion, and reduced physical activity.
A pre-frail state is identified when a patient meets 1 or 2 of these criteria, whereas a frail state is identified when a patient meets more than 2 criteria.
Specifically, grip strength was measured using a Jamar hydraulic dynamometer, the gold standard for grip strength assessment.
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Frailty Idex-Laboratory (FI-laboratory)
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
The FI-Laboratory measures frailty based on routine physical assessments and blood tests based on the accumulation of deficits.
Each item was scored between 0 and 1, with 0 and 1 indicating ideal health and a theoretical state of complete frailty, respectively.
The total score was calculated by dividing the total number of items assessed by the sum of the deficit item scores, with higher scores reflecting increased frailty
|
Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
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Mini-Cog
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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The Mini-Cog, which is used to screen for cognitive issues, comprises 3 components-3-word registration, clock drawing, and 3-word recall-with a maximum score of 5.
One point was assigned for each accurately recalled word (total of 3 points), whereas 2 points were assigned for accurately drawing the clock.
A score of ≤2 indicates the presence of cognitive problems
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
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Patient Health Questionnaire-9 (PHQ-9)
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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The PHQ-9 measures depression and comprises 9 items rated from 0 (not at all) to 3 (nearly every day).
The maximum total score is 27, with scores of 10-19 and 20-27 indicating moderate and severe depression, respectively
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
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Makizako Social Frailty Index
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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The Makizako Social Frailty Index measures social frailty and comprises 5 items, with 2 or more positive responses to questions indicating social frailty.
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
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Heart Failure Frailty Scale (HFFS)
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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The HFFS is a multidimensional frailty assessment instrument that was developed specifically for patients with HF4) and comprises 4 domains.
As of now, no validated cut-off score has been universally established to classify frailty status.
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Kansas City Cardiomyopathy Questionnaire
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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The KCCQ comprises 23 items that quantify 7 domains-physical limitations (6 items), symptom stability (1 item), symptom frequency (4 items), symptom burden (3 items), self-efficacy (2 items), QoL (3 items), and social limitations (4 items)-of health status in patients with HF.
Scores range from 0 to 100, with higher scores indicating better health status and quality of life.
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Worsening Heart Failure events
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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hospitalizations, emergency room visits, and unscheduled visits to outpatients' clinics
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
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Change in NT-proBNP Level from Baseline
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Change in New York Heart Association Functional Class from Baseline
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Assessed by the New York Heart Association (NYHA) Functional Classification, ranging from Class I to Class IV, with higher classes indicating worse functional status.
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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6-minute walk distance
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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|
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changes in muscle mass measured by impedance
Time Frame: Baseline assessment, Post assessment (12 week), Final assessment (24 week)
|
Baseline assessment, Post assessment (12 week), Final assessment (24 week)
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WJC-IIT-1003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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